NTRK Fusion Genes in Thyroid Carcinomas: Clinicopathological Characteristics and Their Impacts on Prognosis
| Autor: | Jana Drozenova, Jitka Moravcova, Jaromír Astl, Petr Hrabal, Barbora Pekova, Eliska Vaclavikova, Miloš Taudy, Petr Lastuvka, Rami Katra, Bela Bendlova, Martin Chovanec, Daniela Kodetova, Vlasta Sykorova, Josef Vcelak, Petr Vlcek, Karolina Mastnikova, Petr Bavor |
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| Jazyk: | angličtina |
| Rok vydání: | 2021 |
| Předmět: |
Neuroblastoma RAS viral oncogene homolog
Cancer Research endocrine system diseases 030209 endocrinology & metabolism medicine.disease_cause Article poorly differentiated thyroid carcinoma Thyroid carcinoma 03 medical and health sciences 0302 clinical medicine Poorly Differentiated Thyroid Carcinoma medicine follow-up HRAS Thyroid cancer RC254-282 business.industry Neoplasms. Tumors. Oncology. Including cancer and carcinogens clinicopathological feature medicine.disease ETV6 Oncology fusion gene 030220 oncology & carcinogenesis Cancer research papillary thyroid carcinoma outcome KRAS prognosis business PAX8 NTRK |
| Zdroj: | Cancers Volume 13 Issue 8 Cancers, Vol 13, Iss 1932, p 1932 (2021) |
| ISSN: | 2072-6694 |
| Popis: | Simple Summary NTRK fusion genes are important but not well studied molecular markers in thyroid cancer. Their identification could help improve diagnosis and prognosis, and determine appropriate treatment. The aims of this study were to identify NTRK fusion-positive thyroid tumors in a large cohort of different thyroid tumors, to characterize these tumors by molecular, clinical and pathological features and to evaluate the impact of NTRK-rearranged tumors on prognosis of the disease. A suitable approach for selective NTRK fusion gene testing in thyroid cancer samples was created and utilized. In a cohort of 59 NTRK-rearranged carcinomas, characteristic features were described and recommendations for surgery and prognostic factors were determined thanks to the long-term follow-up of patients. Abstract Chromosomal rearrangements of NTRK genes are oncogenic driver mutations in thyroid cancer (TC). This study aimed to identify NTRK fusion-positive thyroid tumors and to correlate them with clinical and pathological data and determine their prognostic significance. The cohort consisted of 989 different TC samples. Based on the detected mutation, samples were triaged, and those that were positive for a BRAF, HRAS, KRAS, NRAS, RET, RET/PTC or PAX8/PPARγ mutation were excluded from further analyses. NTRK fusion gene testing was performed in 259 cases, including 126 cases using next-generation sequencing. NTRK fusion genes were detected in 57 of 846 (6.7%) papillary thyroid carcinomas and in 2 of 10 (20.0%) poorly differentiated thyroid carcinomas. A total of eight types of NTRK fusions were found, including ETV6/NTRK3, EML4/NTRK3, RBPMS/NTRK3, SQSTM1/NTRK3, TPM3/NTRK1, IRF2BP2/NTRK1, SQSTM1/NTRK1 and TPR/NTRK1. NTRK fusion-positive carcinomas were associated with the follicular growth pattern, chronic lymphocytic thyroiditis and lymph node metastases. NTRK1-rearranged carcinomas showed a higher frequency of multifocality and aggressivity than NTRK3-rearranged carcinomas. Tumor size, presence of metastases, positivity for the NTRK3 or NTRK1 fusion gene and a late mutation event (TERT or TP53 mutation) were determined as factors affecting patient prognosis. NTRK fusion genes are valuable diagnostic and prognostic markers. |
| Databáze: | OpenAIRE |
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